Synthesis and Insecticidal Activity of Thiacloprid Derivatives against Helicoverpa armigera (Hub)

Madhukar, D. and Sangram, P. and Pandurang, M. and Dasharath, O. and Chetan, S. (2011) Synthesis and Insecticidal Activity of Thiacloprid Derivatives against Helicoverpa armigera (Hub). Pesticide Research Journal, 23 (2). pp. 154-159.

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Abstract

Thiacloprid (1) was converted to the corresponding amide (2) and acid (4) by alkaline hydrolysis. Amide (2) was reacted with phenyl isocynate to give the corresponding urea derivatives (3). The esterification of acid yielded an ester, (5) which was converted to hydrazide (6) with hydrazine hydrate. The thiacloprid was reduced by stannous chloride in dry HCl, and hydrolyzed to get aldehyde (7) and further reduced by Na in absolute alcohol to yield primary amine (8) (Scheme-1). The efficacy of these compounds was studied on Helicoverpa armigera (Hub), the test compound thiacloprid (1.28–1.40%), 6 (1.03–1.21%), 3 (1.25–1.40%), 7 (1.06–1.83%), 8 (0.851.73%) and novaluron (1.51–1.61%) at 200–600 mg L−1, showed higher glycogen content. The amount of protein, lipid and chitin were measured and compared with their chitin inhibition property. Thiacloprid showed the highest mortality (50%, 4th day) at 600 mg L−1.

Item Type: Article
Author Affiliation: Department of Agrochemicals and Pest Management, Shivaji University, Kolhapur 416 004, Maharashtra, India
Subjects: Plant Protection
Divisions: General
Depositing User: Mr. SanatKumar Behera
Date Deposited: 08 Feb 2013 08:43
Last Modified: 08 Feb 2013 08:43
Official URL: http://www.indianjournals.com/ijor.aspx?target=ijo...
URI: http://eprints.icrisat.ac.in/id/eprint/9581

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